The Recall Desk

State

Rhode Island product recalls

73,806 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,054
Critical
221
Severe
708
Most recent
2026-11-04

Of the 3,054 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 708 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40951–40975 of 76860

  • ModerateFDA (Devices)·Z-0889-2018·2018-03-14

    Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades

    Bausch & Lomb is voluntarily recalling 1,236,749 LaserEdge Knives used in ophthalmic surgery because of an atypical volume of complaints regarding dull blades.

    Product
    LASEREDGE Knives, 0.88MM ARROW KNIFE ANGLED (6/BOX), REF/PRODUCT CODE E7593, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0895-2018·2018-03-14

    Instrumentation Laboratory Recalls Hemosll ReadiPlasTin Kits Due to Performance Issues

    Instrumentation Laboratory is recalling 14,894 Hemosll ReadiPlasTin kits due to reported performance issues, including increased imprecision and out-of-range quality controls.

    Product
    Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0577-2018·2018-03-14

    Akorn Recalls Atropine Sulfate Ophthalmic Solution Due to Viscosity Failure

    Akorn, Inc. is recalling 31,812 bottles of Atropine Sulfate Ophthalmic 1% Solution because testing revealed low viscosity results.

    Product
    Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-215-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0585-2018·2018-03-14

    AstraZeneca Recalls Lynparza Capsules Due to Quality Attribute Deviation

    AstraZeneca is recalling 18,056 bottles of Lynparza (olaparib) capsules 50 mg due to elevated levels of a specific quality attribute.

    Product
    Lynparza (olaparib) capsules 50 mg, 112 count bottles, Rx only, Manufactured for: Astra Zeneca Pharmaceuticals LP Wilmington, DE 19850 by: Patheon Pharmaceuticals, Inc. Cincinnati OH 45237 Product of Switzerland NDC 0310-0657-58
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·18120·2018-03-13

    MAAX Spas Recalls Hot Tubs and Swim Spas Due to Fire Hazard

    MAAX Spas is recalling about 550 hot tubs and swim spas in the U.S. because the internal UV generator can ignite, posing a fire hazard.

    Product
    Maax Spas hot tubs and swim spas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18121·2018-03-13

    SwissStop Bicycle Disc Brake Pads Recalled Due to Fall Hazard

    Helvetia Sports is recalling SwissStop EXOTherm cycling disc brake pads because they can separate from the backplate, posing a fall hazard to users.

    Product
    SwissStop EXOTherm cycling disc brake pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V169000·2018-03-12

    Ford Recalls Focus and Fusion Vehicles for Clutch Fracture Risk

    Ford is recalling 2013-2016 Focus and Fusion vehicles with manual transmissions because the clutch may fracture, causing transmission damage and fluid leaks that could lead to fire.

    Product
    FORD — FORD FOCUS, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V163000·2018-03-12

    Freightliner Custom Chassis Recalls 2011-2017 RV Chassis for Fire Risk

    Daimler Trucks North America is recalling 9,480 Freightliner Custom Chassis vehicles due to a power steering hose defect that may cause electrical arcing and fire.

    Product
    FCCC — FCCC XCM, XBR, XCL, XCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V167000·2018-03-12

    Ford Recalls 2014-2018 Fusion and Lincoln MKZ for Steering Wheel Defect

    Ford is recalling 2014-2018 Fusion and Lincoln MKZ vehicles because the steering wheel bolt may loosen, allowing the wheel to detach and causing loss of control.

    Product
    FORD — FORD, LINCOLN FUSION, MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E015000·2018-03-09

    SynTec Recalls S3B School Bus Seats Due to Bracket Crack Risk

    SynTec Seating Solutions is recalling S3B Non-Restraint Wall Mounted Seats because the mounting bracket may crack, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V162000·2018-03-09

    Forest River Recalls 2018 Stealth Evo Trailers for Incorrect Tire Placards

    Forest River is recalling 2018 Stealth Evo recreational trailers because the federal placard lists incorrect tire sizes. This error could lead owners to install wrong replacement tires, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V164000·2018-03-09

    Ferrari Recalls 2016 488 GTB and Spider for Brake Warning Software Error

    Ferrari is recalling 2016 488 GTB and 488 Spider vehicles because a software error may prevent drivers from receiving warnings about critically worn brake discs.

    Product
    FERRARI — FERRARI 488 GTB, 488 SPIDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V168000·2018-03-09

    Supreme Trucks Recalled for Defective Kidde Fire Extinguishers

    Supreme Corporation is recalling 2003-2018 trucks equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks during a fire.

    Product
    SUPREME — SUPREME SIGNATURE VAN, SERVICE BODY, KOLD KING, INER-CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V160000·2018-03-08

    Dodge Ram 1500 Fuel Tank Strap Corrosion Recall

    Chrysler is recalling 2009-2012 Dodge Ram 1500 trucks in 21 states and D.C. because a fuel tank bracket may corrode, causing the tank to drop and leak fuel.

    Product
    DODGE — DODGE, RAM RAM 1500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V159000·2018-03-08

    Volkswagen Recalls 2018 Tiguan Models Due to Engine Support Bolt Issue

    Volkswagen is recalling 2018 Tiguan long wheel base vehicles because engine support bolts may not be properly tightened, which could lead to engine breakdown or loss of power.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18727·2018-03-08

    Golden State Warriors Menorahs Recalled Due to Fire and Burn Hazards

    BDA is recalling Golden State Warriors Menorahs because the glue holding the candleholders can melt, causing lit candles to fall and posing fire and burn risks.

    Product
    Golden State Warriors Menorahs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18E014000·2018-03-08

    ATC Recalls 7-Way Wiring Harnesses for Truck Caps Due to Fire Risk

    American Technology Components is recalling specific 7-Way Wiring Harnesses used for aftermarket truck cap installations because the wiring may overheat, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0574-2018·2018-03-07

    AuroMedics Recalls Levofloxacin Injection Bags Due to Mold Contamination

    AuroMedics Pharma LLC is recalling 6,072 bags of Levofloxacin in 5% Dextrose Injection because they contain visible particulate matter identified as mold.

    Product
    LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN IN 5% DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0551-2018·2018-03-07

    Kareway Recalls Gericare Eyewash Due to Confirmed Microbial Contamination

    Kareway Products Inc. is recalling 60,000 bottles of Gericare Eyewash because testing confirmed the presence of Achromobacter xylosoxidans bacteria.

    Product
    GERICARE Eyewash, sterile eye irrigating solution, packaged in a 4 fl oz (118 mL) bottle, OTC, Distributed by Geri-Care Pharmaceuticals Corp., Brooklyn, NY 11204, NDC 57896-0186-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0923-2018·2018-03-07

    Seggiano Artichoke & Garlic Sauce Recalled for Undeclared Cashews

    Seggiano Artichoke & Garlic Sauce & Spread is being recalled because it was mislabeled and contains undeclared cashews.

    Product
    Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381
    Category
    Food
    Distribution
    Distributed nationwide